The invention relates to a continuous process for removing salts in the course of preparation of dimethylacetamide.
Dimethylacetamide (DMAC) finds use as a polar solvent, especially for polymers and gases, as a stripping agent, extractant and crystallization auxiliary. In the paints industry, DMAC, because of its high boiling temperature, is used for specific coating materials based on polymeric binders, especially polyamides and polyurethanes. DMAC additionally finds use for production of fibers and films and as a reaction medium. DMAC can be used as an auxiliary in the spinning of Spandex® fibers and can subsequently also be at least partly recovered.
WO 2006/061159 A1 discloses a continuous process for preparing N,N-dimethylacetamide (DMAC) by continuous reaction of methyl acetate (MeOAc) with dimethylamine (DMA) in the presence of a basic catalyst. The catalyst is in homogeneous and/or suspended form in the reaction mixture. When methanolic MeOAC solution is used, as obtained in the preparation of polytetrahydrofuran (poly-THF), it is also possible for by-products to be present. These by-products may especially be tetrahydrofuran (THF) and/or dimethyl ether. The liquid reaction outputs from the process can be decompressed in a distillation column for further workup.
Preferably, the basic catalyst present in the reaction output is neutralized. This is accomplished by addition especially of water or an aqueous or anhydrous protic acid, especially sulfuric acid, methanesulfonic acid, carboxylic acid, phosphoric acid and the like.
WO 2006/061159 A1 discloses a removal of salts from the reaction output by evaporation.
A disadvantage in this process is growing encrustation with increasing operating time, especially crystallization fouling and caking, especially on heated walls, which results in lower heat transfer performance, and also in blockage of pipelines and in that case ultimately a time-consuming and material-intensive exchange of system elements. The exchange of the system elements causes maintenance shutdowns with production shutdown periods, and also a high expenditure of material and the associated costs.
A further disadvantage is the cleaning and processing of the exchanged system elements. The time-consuming cleaning operation additionally gives rise to salt-containing wastewaters which may especially also contain residual amounts of DMAC, which, in addition to discontinuous occurrence of highly concentrated wastewater in a wastewater cleaning system, can lead to further problems.
It was therefore an object of the invention to provide an improved process which overcomes the above disadvantages.
The object is achieved by a continuous process for discharging a solid, salt-containing phase comprising alkali metal acetates and/or alkaline earth metal acetates from the product mixture from the preparation of N,N-dimethylacetamide (DMAC) by reaction of methyl acetate (MeOAc) with dimethylamine (DMA) in the presence of a catalyst comprising N,N-dimethylacetamide (DMAC), methyl acetate (MeOAc), dimethylamine (DMA) and a catalyst, having the following process steps:
level-regulated feeding of the product mixture as feed stream into an evaporation vessel of a forced circulation evaporator, where the forced circulation evaporator has, in flow direction, at least one evaporation vessel, a pump, a first heat exchanger and a recycle line into the evaporation vessel as a forced circulation evaporation circuit, where the recycle line has a throttle element and, disposed at the end in flow direction, an introduction section, where the level-regulated feeding of the product mixture is used for closed-loop control of a defined fill level in the evaporation vessel, where the product mixture at their defined fill level of the evaporation vessel has a level surface,
flash evaporation of volatile components of the product mixture in the forced circulation evaporator to form a vapor phase comprising N,N-dimethylacetamide (DMAC) and precipitation of a solid, salt-containing phase comprising alkali metal acetates and/or alkaline earth metal acetates,
recycling of the volatile components of the product mixture obtained in the vapor phase after the flash evaporation, of any unevaporated components of the product mixture in the liquid phase and of the solid, salt-containing phase comprising alkali metal acetates and/or alkaline earth metal acetates into the evaporation vessel via the recycle line,
removal of the vapor phase comprising N,N-dimethylacetamide (DMAC) from the evaporation vessel as output stream,
concentration of the solid, salt-containing phase comprising alkali metal acetates and/or alkaline earth metal acetates in the forced circulation evaporation circuit of the forced circulation evaporator,
discharge of a substream comprising the solid, salt-containing phase comprising alkali metal acetates and/or alkaline earth metal acetates from the forced circulation evaporation circuit of the forced circulation evaporator,
solid/liquid separation of the discharged substream comprising the solid, salt-containing phase comprising alkali metal acetates and/or alkaline earth metal acetates in at least one separation apparatus into a solid, salt-containing phase comprising alkali metal acetates and/or alkaline earth metal acetates and a liquid phase,
recycling of the liquid phase obtained after the solid/liquid separation into the forced circulation evaporation circuit as recycle stream,
wherein the recycling of the volatile components of the product mixture obtained after the flash evaporation and of the solid, salt-containing phase comprising alkali metal acetates and/or alkaline earth metal acetates into the evaporation vessel via the recycle line is effected via an introduction section which ends within a range from 30 cm above the level surface to 20 cm below the level surface of the fill level of the evaporation vessel.
Level-regulated feeding of the product mixture in the context of present invention is understood to mean feeding of the product mixture into the evaporation vessel which is regulated as a function of a defined level in the evaporation vessel. If the level in the evaporation vessel is below the defined level, product mixture in particular is fed in until the defined level is attained.
A feed stream in the context of the present invention is in principle understood to mean any desired feed stream which supplies the process with starting raw material(s) in particular.
A forced circulation evaporator in the context of the present invention is understood to mean a circulation evaporator which utilizes a pump in particular in order to force the product mixture comprising volatile components to flow through the circulation evaporator. The forced circulation evaporation circuit is formed in flow direction by the evaporation vessel, the pump, the first heat exchanger and the recycle line into the evaporation vessel.
A recycle line in the context of the present invention is understood to mean a line which, in the forced circulation evaporation circuit, in flow direction, leads back from the first heat exchanger into the evaporation vessel. The recycle line may especially be a pipe, a hose.
A throttle element in the context of the present invention is understood to mean any device which generates a pressure differential in the recycle line from the upstream side to the downstream side of the throttle element in flow direction, the pressure in the recycle line being higher upstream of the throttle element in flow direction than the pressure downstream of the throttle element in flow direction, such that decompression takes place downstream of the throttle element in flow direction.
An introduction section in the context of the present invention is understood to mean any device through which volatile components of the product mixture obtained after the flash evaporation, any unevaporated components of the product mixture in a liquid phase and a solid, salt-containing phase comprising alkali metal acetates and/or alkaline earth metal acetates is introduced into the evaporation vessel via the recycle line. The introduction section may especially be a pipe section, a nozzle, a hose.
Recycling of the volatile components of the product mixture obtained after the flash evaporation in the context of present invention is understood to mean the recycling of components of the product mixture from the forced circulation evaporation circuit into the evaporation vessel. The recycling may especially be effected downstream of the throttle element in the recycle line through the introduction section.
Recycling of the liquid phase obtained after the solid/liquid separation in the context of present invention is understood to mean the recycling of the liquid phase obtained after the solid/liquid separation into the evaporation vessel. Recycling of components into the evaporation vessel fundamentally also affects the fill level of the evaporation vessel.
A defined fill level in the context of the present invention is understood to mean a defined fill height in the evaporation vessel. The defined fill level is affected especially by the feeding of the product mixture, the removal of the vapor phase and the discharge of a substream. The definition of the fill level is determined by the distance between the level surface of the fill level and the introduction section.
Level surface in the context of the present invention is understood to mean the level surface at the fill height in the evaporation vessel. The level surface may especially be the outer surface of a liquid phase, or of a foam phase, at the fill height in the evaporation vessel.
Separation apparatus in the context of present invention is in principle understood to mean any apparatus for separation of liquid and solid phases. The separation can especially be effected by means of filtration, especially cake-forming filtration, cartridge filtration, membrane filtration, ultrafiltration, surface filtration, depth filtration, centrifugal processes, screening processes, sedimentation processes in the earth's gravitational field or a centrifugal field.
An advantageous processes a continuous process in which the product mixture in the recycle line, downstream of the throttle element in flow direction, has a flow rate within a range from 0.5 to 4 m/s. Preference is given to flow rates of 1-3 m/s, particular preference to those in the range of 1.5-2.5 m/s.
Preferably, the product mixture in the recycle line, downstream of the throttle element in the continuous process, has a temperature in the range from 50 to 300° C. Preference is given to temperatures in the range of 80-250° C., particular preference to those in the range of 100-250° C.
Preferably, in the continuous process, the product mixture leaving the introduction section has a flow having a Reynolds number greater than 104.
Preferably, in the continuous process, the product mixture comprising N,N-dimethylacetamide (DMAC) in the recycle line, downstream of the throttle element in flow direction, has such a pressure/temperature relationship that N,N-dimethylacetamide (DMAC) is in the vapor phase.
Preferably, the removed vapor phase is distilled by cooling in at least one second heat exchanger to obtain N,N-dimethylacetamide (DMAC).
Preferably, the throttle element in the continuous process is a pressure-retaining unit, a valve, a regulating valve, a slide valve, a diaphragm, a ring diaphragm, a nozzle, a flap, a pipe constriction, a hole or else a combination thereof.
Preferably, the throttle element in the continuous process is set up such that a pressure differential in a region upstream of the throttle element to a region downstream of the throttle element in flow direction is preferably greater than 0.1 bar.
Preferably, the evaporation for removal of salt in the evaporation vessel has a pressure in the range of 0.01-5 bar, more preferably in the range of 0.1-2 bar.
Preferably, the vapor phase removed from the evaporation vessel in the continuous process has a proportion in the range from 30% to 99% by weight of N,N-dimethylacetamide (DMAC), based on the total weight of the feed stream.
Preference is given to processes in which 50%-99%, more preferably 90%-99%, based on the total weight of the feed stream, is evaporated. Nonvolatile compounds and salt remain in the residue.
Preferably, the process is conducted continuously and especially has a mean residence time of the product of value in the range of 1-60 minutes, more preferably in the range of 30-60 minutes.
Preferably, the flash evaporation in the continuous process comprises a plurality of evaporation apparatuses arranged in series, in parallel, or in combinations thereof.
In a suitable configuration, the evaporation comprises a plurality of forced circulation evaporators arranged in series, in parallel or in combination thereof. The connection system of the forced circulation evaporators may comprise, for example, two to twelve, preferably two to ten and especially two, three, four, five or six, identical or different forced circulation evaporators. The forced circulation evaporators may each be operated with or without recycling. The output from one forced circulation evaporator may also be conducted at least partly into an upstream forced circulation evaporator.
Preferably, the flash evaporation takes place in one stage or a plurality of successive stages, for example in two, three, four, five or six successive stages.
The solid/liquid separation in the continuous process is a filtration, especially a cake-forming filtration, a cartridge filtration, a membrane filtration, an ultrafiltration, a surface filtration, a depth filtration, a centrifugal process, a screening process, a sedimentation process in the earth's gravitational field and/or a centrifugal field, or else combinations thereof.
The solid/liquid separation in the continuous process is continuous or batchwise.
The catalyst in the continuous process is a basic catalyst, alkali metal hydroxide, alkaline earth metal hydroxide, alkali metal alkoxide, alkaline earth metal alkoxide, alkali metal carbonate, alkaline earth metal carbonate, alkali metal hydrogencarbonate, alkaline earth metal hydrogencarbonate, an amine, especially a tertiary amine, and combinations thereof, and the alkali metal is Li, Na, K, Rb, Cs and combinations thereof.
The evaporation of the continuous process has a specific heating surface load in the range of 1-100 kW/m2, based on the heating output transferred and the evaporator surface area of the evaporator.
Preference is given to a heating surface load in the range of 10-80 kW/m2, most preferably in the range of 20-40 kW/m2.
Preferably, the heat exchanger is heated by means of heating steam or heat carrier medium.
The process according to the invention has the following advantages:
The invention is elucidated in detail hereinafter by a working example and a drawing.
The following reference symbols are used:
The schematic overview diagram in
A preferred plant for performing the process according to the invention may have a plurality of forced circulation flash evaporators arranged in a cascade connection. In a cascade connection, forced circulation flash evaporators are arranged such that a residue from a first forced circulation flash evaporator is passed into a second forced circulation flash evaporator and the residue from the second forced circulation flash evaporator is passed into a third forced circulation flash evaporator, which is continued further with a further number of forced circulation flash evaporators. In the case of a plurality of evaporator stages, the vapors from the upstream evaporator stage are used to heat the downstream evaporator stage. Preferably, the vapors can also be sent to a distillation column.
Preferably, there is no formation of vapor bubbles when the product mixture is heated in the first heat exchanger W1. In this way, it is possible to avoid precipitation and the caking of solids that have a tendency to form crusts on heated walls. Vapor bubble formation does not take place until downstream of the throttle element D, especially a pressure-retaining valve, in flow direction.
Preferably, a separation is effected in the separation apparatus T by the customary processes, especially with cartridge filters. In this case, it is possible with preference to use an open filter fabric made from Teflon having an air passage rate of 150 L/dm2/min.
If the filtercake resistance becomes too high, the feed is stopped and the filtercake is cleaned further to remove organic residues by blowing with nitrogen or steam before the filtercake is either disposed of or the salt is dissolved with water and sent to a water treatment plant.
An advantage of using steam for the blowing-dry operation is the option of condensing the steam obtained with the organic material. The water obtained can then be used for catalyst breakdown and enables recycling of the organic material. In the case of use of nitrogen, the stream would have to be disposed of by means of a flare.
The output which has been evaporated off the solids and partially or totally condensed is worked up by distillation under the customary distillation conditions, for example in one or more columns connected to one another.
The pilot plant comprised a forced circulation evaporator, a downstream distillation column and a solid/liquid separation apparatus. In the circuit of the forced circulation evaporator, in flow direction, an evaporation vessel V, a centrifugal pump P, a first heat exchanger W1 and a recycle line R the evaporation vessel V. Disposed downstream of the first heat exchanger W1 in the recycle line R was a throttle element D and, at the end in flow direction, an introduction section E. As feed stream 1, a product mixture was fed under level control into the evaporation vessel V. The product mixture was produced according to WO 2006/061159 A1, consisting of 15% by weight of methanol, 3% by weight of dimethylamine, 6% by weight of methyl acetate, 75% by weight of DMAC and about 1% by weight of sodium methoxide. 1% by weight of water was added continuously to the product mixture, based on the feed stream 1, in order to neutralize sodium methoxide, and the product mixture was conveyed under level control into the evaporation vessel V, in order to form a fill level N in the evaporation vessel having a level surface O. From the evaporation vessel V, the product mixture was pumped into the first heat exchanger W1 with a centrifugal pump P and heated to a temperature in the range from 120° C. to 150° C. The first heat exchanger W1 was heated by means of a heat carrier oil. The specific heating surface output was 20 kW/m2.
The pumping of the product mixture through the first heat exchanger W1 in flow direction against a throttle element D built up a pressure in the first heat exchanger W1. This pressure in the heat exchanger was regulated with the throttle element, especially a regulating valve in the outlet region of the heat exchanger W1, and adjusted such that there was no vapor bubble formation and no evaporation in the heat exchanger W1 during the heating of the product mixture. The throttle element D was adjusted such that there is a pressure differential between the pressure within the heat exchanger and the pressure downstream of the throttle element D in flow direction within a range from 0.1 to 0.5 bar, with a drop in the pressure downstream of the throttle element in flow direction. The pressure in the evaporation vessel was in the range from 0.5 to 1.2 bar.
Downstream of the throttle element in flow direction, the volatile components of the product mixture were flash-evaporated to form a vapor phase F comprising N,N-dimethylacetamide (DMAC) and precipitate a solid, salt-containing phase comprising especially sodium acetate. The vapor phase F especially also comprises the components of the product mixture and may comprise, for example, about 15% by weight of methanol, about 3% by weight of dimethylamine, about 6% by weight of methyl acetate, about 75% by weight of DMAC, about 1% by weight of water, based on the total weight of the product mixture. The volatile components of the product mixture obtained after the flash evaporation, any unevaporated components of the product mixture in a liquid phase and a solid, salt-containing phase were recycled into the evaporation vessel through the recycle line R via the introduction section E. The flow rate in the recycle line R downstream of the throttle element D in flow direction was 2 m/s. The introduction section was adjusted such that it ends within a region from 30 cm immediately above to 20 cm below the level surface O of the fill level N of the evaporation vessel. The vapor phase was removed from the evaporation vessel as output stream 2 and condensed in the second heat exchanger W2. The evaporating operation and the removal of the vapor phase resulted in concentration of the solid, salt-containing phase in the evaporation vessel V. Concentrations up to a range of more than 80% by weight, preferably of more than 50% by weight, based on the total weight of the product mixture are possible. Over and above a salt concentration of 25% by weight, based on the total weight of the product mixture in the evaporation vessel V, a substream 3 was discharged from the evaporation vessel V under level control and fed to a solid/liquid separation apparatus T configured as a suction filter. After the solids had been separated from the liquid, the liquid was fed back to the evaporation, especially the evaporation vessel V. During the continuous three-week experiment, no solid deposits were found in the pipelines of the first heat exchanger W1. No cleaning of the pilot plant during the test period was necessary.
Number | Date | Country | Kind |
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12197998.3 | Dec 2012 | EP | regional |
Filing Document | Filing Date | Country | Kind |
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PCT/EP2013/077087 | 12/18/2013 | WO | 00 |